Ricks-Santi Luisel J, Fredenburg Kristianna, Rajaei Moein, Esnakula Ashwin, Naab Tammey, McDonald J Tyson, Kanaan Yasmine
Department of Pharmacotherapy and Translational Research, College of Pharmacy, University of Florida, Gainesville, FL.
Department of Pathology, College of Medicine, University of Florida, Gainesville, FL.
Res Sq. 2023 Jan 25:rs.3.rs-2463961. doi: 10.21203/rs.3.rs-2463961/v1.
GATA3 and Mammaglobin are often used in the clinic to identify metastases of mammary origin due to their robust and diffuse expression in mammary tissue. However, the expression of these markers has not been well characterized in tumors from African American women. The goal of this study was to characterize and evaluate the expression of GATA3 and mammaglobin breast tumors from African American women and determine their association with clinicopathological outcomes including breast cancer subtypes. Tissue microarrays (TMAs) were constructed from well preserved, morphologically representative tumors in archived formalin-fixed, paraffin-embedded (FFPE) surgical blocks from 202 patients with primary invasive ductal carcinoma. Mammaglobin, and GATA3 expression was assessed using immunohistochemistry (IHC). Univariate analysis was carried out to determine the association between expression of GATA3, mammaglobin and clinicopathological characteristics. Kaplan-Meier estimates of overall survival and disease-free survival were also plotted and a log-rank test performed to compare estimates among groups. GATA3 expression showed statistically significant association with lower grade (p<0.001), ER-positivity (p<0.001), PR-positivity (p<0.001), and the luminal subtype (p<0.001). Mammaglobin expression was also significantly associated with lower grade (p=0.031), ER-positivity (p=0.007), and PR-positivity (p=0.022). There was no association with recurrence-free or overall survival. Our results confirm that GATA3 and mammaglobin demonstrate expression predominantly in luminal breast cancers from African American women. Markers with improved specificity and sensitivity are warranted given the high prevalence of triple negative breast cancer in the group.
GATA3和乳腺珠蛋白在临床上常被用于识别乳腺来源的转移灶,因为它们在乳腺组织中表达强烈且广泛。然而,这些标志物在非裔美国女性肿瘤中的表达尚未得到充分表征。本研究的目的是表征和评估非裔美国女性乳腺肿瘤中GATA3和乳腺珠蛋白的表达,并确定它们与包括乳腺癌亚型在内的临床病理结果之间的关联。组织微阵列(TMA)由202例原发性浸润性导管癌患者存档的福尔马林固定、石蜡包埋(FFPE)手术块中保存良好、形态学代表性的肿瘤构建而成。使用免疫组织化学(IHC)评估乳腺珠蛋白和GATA3的表达。进行单因素分析以确定GATA3、乳腺珠蛋白表达与临床病理特征之间的关联。还绘制了总生存和无病生存的Kaplan-Meier估计值,并进行对数秩检验以比较各组之间的估计值。GATA3表达与低级别(p<0.001)、雌激素受体阳性(p<0.001)、孕激素受体阳性(p<0.001)和管腔亚型(p<0.001)显示出统计学上的显著关联。乳腺珠蛋白表达也与低级别(p=0.031)、雌激素受体阳性(p=0.007)和孕激素受体阳性(p=0.022)显著相关。与无复发生存或总生存无关联。我们的结果证实,GATA3和乳腺珠蛋白主要在非裔美国女性的管腔型乳腺癌中表达。鉴于该组三阴性乳腺癌的高患病率,需要具有更高特异性和敏感性的标志物。